Synthetic studies in cinnamylated derivatives of resacetophenone and related compounds

1978 ◽  
Vol 87 (6) ◽  
pp. 189-198
Author(s):  
A C Jain ◽  
A Kumar ◽  
R C Gupta
1968 ◽  
Vol 46 (7) ◽  
pp. 1079-1091 ◽  
Author(s):  
Joseph Zauhar ◽  
Benoit F. Ladouceur

The reactions of several substituted 5-chloropyrazoles with hydrazine hydrate and guanidine, respectively, were investigated in ethanol and dimethyl formamide media. In certain cases, only SN2 reactions occurred, while in others the 5-hydrazino- and 5-guanidopyrazoles reacted still further to yield related compounds with two pyrazole rings. On the basis of the intermediates and the different condensation products isolated, reaction schemes are proposed for the reactions discussed.


ChemInform ◽  
2010 ◽  
Vol 24 (9) ◽  
pp. no-no
Author(s):  
M. TANI ◽  
H. IKEGAMI ◽  
M. TASHIRO ◽  
T. HIURA ◽  
H. TSUKIOKA ◽  
...  

Heterocycles ◽  
1992 ◽  
Vol 34 (12) ◽  
pp. 2349 ◽  
Author(s):  
Yasuoki Murakami ◽  
Masanobu Tani ◽  
Hiroyo Ikegami ◽  
Mayumi Tashiro ◽  
Tetsuji Hiura ◽  
...  

1976 ◽  
Vol 29 (10) ◽  
pp. 2247 ◽  
Author(s):  
HJ Banks ◽  
DW Cameron ◽  
MJ Crossley ◽  
EL Samuel

5,7-Dihydroxy-2,3-dimethyl-l,4-naphthoquinone (5) and related compounds have been synthesized. The quinone affords an accessible substrate for studying an unusual reaction with nucleophiles, which involves attack at the 8-position, i.e. at the benzenoid ring. An unsuccessful approach to (5) has led to tri- and tetra-nitro derivatives of 2,3-dimethylnaphthalene. Reduction of the former and subsequent conversions have given aminonaphthoquinone and perimidinone derivatives.


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